A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15767477



Internal ID22101953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18116767..18116767hg38UCSC Ensembl
chr19:18227577..18227577hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4441598
Supporting Variants
Samples
Known GenesMAST3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15767477
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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